Certificate Course in Drug Regulatory Affairs (DRA)

Overview

Drug regulatory affairs is a field of healthcare that deals with the regulation of drugs. It ensures that drugs are safe for use and meet quality standards. Drug regulatory affairs also ensure that the appropriate clinical trials are conducted and that drug labels are accurate and up-to-date. Drug regulatory affairs are the process of ensuring that a drug or medical device complies with all the applicable laws and regulations before it can be marketed. Drug safety is the most important aspect of drug regulatory affairs as it ensures that drugs are safe for consumption.

Course Objectives:  

• The objective of drug regulatory affairs courses is to provide the knowledge and skills necessary for those who are interested in the work of the pharmaceutical industry. 
• These courses provide information on how to work in a regulatory affairs department, how drugs are regulated and marketed, and what careers are available in this field. 
• Drug regulatory affairs courses provide an overview of the various topics that are related to drug regulation and the course will also provide information on how these topics can be applied in daily life.

Timing for Webinar: 3 pm to 5 pm (2 hours weekly on Sunday)
 

Eligibility

This course can be enrolled by any life science, Pharma graduate, and postgraduate student including MBBS, BDS, BAMS, B. Pharm, M. Pharm, B.Sc., M.Sc., Life science, Nursing and all professionals working with Hospitals & Healthcare Organizations can apply for this course.

 

Minimum Education